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Salmonella-Infected Aortic Aneurysm: Investigating Pathogenesis Using Salmonella Serotypes

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Salmonella-Infected Aortic Aneurysm: Investigating Pathogenesis Using Salmonella Serotypes Polish Journal of Microbiology ORIGINAL PAPER 2019, Vol. 68, No 4, 439–447 https://doi.org/10.33073/pjm-2019-043 Salmonella-Infected Aortic Aneurysm: Investigating Pathogenesis Using Salmonella Serotypes CHISHIH CHU1, MIN YI WONG2, CHENG-HSUN CHIU3,4, YUAN-HSI TSENG2, CHYI-LIANG CHEN3 and YAO-KUANG HUANG2* 1 Department of Microbiology, Immunology, and Biopharmaceuticals, National Chiayi University, Chiayi, Taiwan 2 Division of Thoracic and Cardiovascular Surgery, Chiayi Chang Gung Memorial Hospital, Chiayi, and College of Medicine, Chang Gung University, Taoyuan, Taiwan 3 Molecular Infectious Disease Research Center, Chang Gung Memorial Hospital, Taoyuan, Taiwan 4 Division of Pediatric Infectious Diseases, Department of Pediatrics, Chang Gung Children’s Hospital and Chang Gung University, Taoyuan, Taiwan Submitted 17 April 2019, revised 15 August 2019, accepted 19 August 2019 Abstract Salmonella infection is most common in patients with infected aortic aneurysm, especially in Asia. When the aortic wall is heavily athero- sclerotic, the intima is vulnerable to invasion by Salmonella, leading to the development of infected aortic aneurysm. By using THP-1 macrophage-derived foam cells to mimic atherosclerosis, we investigated the role of three Salmonella enterica serotypes – Typhimurium, Enteritidis, and Choleraesuis – in foam cell autophagy and inflammasome formation. Herein, we provide possible pathogenesis ofSalmo - nella-associated infected aortic aneurysms. Three S. enterica serotypes with or without virulence plasmid were studied. Through Western blotting, we investigated cell autophagy induction and inflammasome formation inSalmonella -infected THP-1 macrophage-derived foam cells, detected CD36 expression after Salmonella infection through flow cytometry, and measured interleukin (IL)-1β, IL-12, and interferon (IFN)-α levels through enzyme-linked immunosorbent assay. At 0.5 h after infection, plasmid-bearingS . Enteritidis OU7130 induced the highest foam cell autophagy – significantly higher than that induced by plasmid-less OU7067. However, plasmid-bearing S. Choleraesuis induced less foam cell autophagy than did its plasmid-less strain. In foam cells, plasmid-less Salmonella infection (particularly S. Cholerae- suis OU7266 infection) led to higher CD36 expression than did plasmid-bearing strains infection. OU7130 and OU7266 infection induced the highest IL-1β secretion. OU7067-infected foam cells secreted the highest IL-12p35 level. Plasmid-bearing S. Typhimurium OU5045 induced a higher IFN-α level than did other Salmonella serotypes. Salmonella serotypes are correlated with foam cell autophagy and IL-1β secretion. Salmonella may affect the course of foam cells formation, or even aortic aneurysm, through autophagy. Key words: Salmonella serotype, virulence plasmid, foam cell, autophagy, inflammasome Introduction takes up oxidized low-density lipoprotein (oxLDL) via type B scavenger receptors CD36 and scavenger recep- A healthy aortic wall is highly resistant to infection. tor-A (SR-A), leading to cholesterol-laden foam cell However, when its intima is diseased, such as in patients formation (Bekkering et al. 2014). with atherosclerosis, the wall becomes susceptible to Autophagy is an evolutionarily conserved process infection. Salmonella, the most common genus of the involved in bulk degradation of long-lived proteins pathogen associated with infected aortic aneurysms, and organelles through which these cytoplasmic com- often infects preexisting atherosclerotic aortic aneu- ponents are sequestered within double-membrane vesi- rysms. Atherosclerosis is a chronic inflammatory, lipid- cles, namely autophagosome followed by lysosomal deg- driven disease. The formation of macrophage foam cells radation (Nishida et al. 2008; Martinet and De Meyer in the arterial intima is a known hallmark of early-stage 2009). In general, this catabolic process is mediated by atherosclerosis lesions (Yu et al. 2013). Within the inti- numerous autophagy and autophagy-related proteins. mal layer, monocyte-derived macrophage subsequently Two conjugation systems, Atg12-conjugation, and LC3 * Corresponding author: Y.-K. Huang, Division of Thoracic and Cardiovascular Surgery, Chiayi Chang Gung Memorial Hospital, Chiayi and College of Medicine, Chang Gung University, Taoyuan, Taiwan; [email protected] © 2019 Chishih Chu et al. This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 License (https://creativecommons. org/licenses/by-nc-nd/4.0/).0 440 Chu Ch. et al. 4 (microtubule-associated protein light chain 3)-lipida- Huang et al. 2014b). In this study, we investigate the role tion are essential for the dynamic process of autophago - of different serotypes ofSalmonella enterica, including some formation (Vural and Kehrl 2014). The conjugate Typhimurium, Enteritidis, and Choleraesuis in foam of a phosphatidylethanolamine group to the carboxyl cells autophagy and inflammasome during infection, terminus of LC3-I to generate LC3-II, localized to outer and we provide possible pathogenesis of Salmonella- and inner autophagosomal membranes, is useful as an associated infected aortic aneurysms. autophagosomal marker. Inflammasomes are important intracellular mul- tiprotein complexes consisting of a cytosolic sensor Experimental belonging to the AIM2 (absent in melanoma 2), or NLR (NOD-like receptors), an adaptor protein ASC Materials and Methods (an apoptosis-associated speck-like protein contain- ing a CARD), and an effector caspase, primarily cas- Bacterial strains and growth conditions. The bac- pase-1. Inflammasomes which regulate the processing terial strains used in this study are listed in Table I. The and releasing of mature pro-inflammatory cytokines wild type strains of S. enterica serovar Typhimurium interleukin-1β (IL-1β) and IL-18, are activated by OU5045, S. enterica serovar Enteritidis OU7130, and a variety of PAMPs and DAMPs (Martinon et al. 2002). S. enterica serovar Choleraesuis OU7085 carried 90-, Caspase-1, caspase-4, and caspase-5 in humans are the 60-, and 50-kb virulence plasmids, respectively. We also inflammatory caspases that are activated through the used strains without a virulence plasmid: S. Typhimu- stimulation of either the NLRC4 or NLRP3 inflamma- rium OU5046, S. Enteritidis OU7067, and S. Chole- some (Martinon and Tschopp 2007). In response to raesuis OU7266. All bacterial strains used in this study bacterial infection, NLRP3 and NLRC4 inflammasomes were routinely grown on xylose lysine deoxycholate can lead to autocatalytic cleavage of caspase-1, followed agar plate, and every single black colony was later by secretion of IL-1β and IL-18 resulting in pyroptosis grown in Luria-Bertani (LB) broth at 37°C overnight. (Bergsbaken et al. 2009). Autophagy and inflammasome Cell culture and differentiation.The monocyte-like are functionally interconnected; they both control cell THP-1 cell line that derived from the peripheral blood homeostatic processes such as critically control inflam- of a childhood case of acute monocytic leukemia was mation and the clearance of pathogens (Seveau et al. obtained from the Bioresource Collection and Research 2018). Autophagy can directly regulate IL-1β activation, Center, Taiwan. The cells were grown in RPMI 1640 release, and signaling that are activated by inflamma- (Sigma Aldrich, St. Louis, MO, R6504) supplemented some (Sun et al. 2017; Wang et al. 2018). with 10% preheated fetal bovine serum (FBS; Sigma Salmonella species are the most common pathogens Aldrich, St. Louis, MO), 2 mM L-glutamine (Sigma of infected aortic aneurysm in Asia. Salmonella-asso- Aldrich, St. Louis, MO, G7513), and 1% penicillin-strep- ciated infected aortic aneurysms have a more favorable tomycin (Sigma Aldrich, St. Louis, MO, P0781). The therapeutic response to endovascular repair compared cells were cultured at 37°C in 5% CO2 and 70% humid- with those associated with other organisms (e.g., Staph- ity. The culture medium was changed every 3–4 days. ylococcus, Streptococcus, and Enterococcus). We previ- The cell density was maintained between 2 × 105 and ously demonstrated that different serotypes ofSalmo - 1 × 106 cells/ml. Furthermore, 5 × 106 THP-1 cells/10 ml nella may affect clinical outcomes (Huang et al. 2014a). were seeded in a 10-cm dish and differentiated using The link to atherosclerosis and its more favorable 10–5 M phorbol myristate acetate (PMA; Sigma Aldrich, response to endovascular aortic repair are implicated St. Louis, MO, P8139) for 48 h at 37°C in 5% CO2. For in the unique pathogenesis of Salmonella-associated foam cell preparation, the differentiated THP-1 cells infected aortic aneurysms (Forbes and Harding 2006; were treated with 50 μg/ml oxLDL (Biomedical Techno- Table I Characteristics of S. Typhimurium, S. Enteritidis, and S. Choleraesuis strains. Serovars Strains Characteristics of virulence plasmid S. Typhimurium OU5045 With a 90-kb pSTV as a wild type OU5046 Without pSTV from wild type S. Enteritidis OU7130 With a 60-kb pSEV as a wild type OU7067 Without pSEV from wild type S. Choleraesuis OU7085 With a 50-kb pSCV as a wild type OU7266 Without pSCV from wild type 4 Foam cells autophagy by Salmonella infection 441 logies Inc., BT-910) for 24 h, and oil red O staining was cial ECL reagents (GE Healthcare Life Sciences) and performed to confirm foam cell formation. exposed to photographic film. Detection of CD36 expression. To detect cell sur- Statistical analysis. Statistical analyses were per- face expression of CD36, flow cytometric analysis
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